Clinical Research Associate II or Senior
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What you'll do
- Monitor clinical trial sites through on‑site and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with cross‑functional teams to meet project timelines
- Manage site‑level study documentation, systems updates, and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
What they're looking for
- Fluent in English and Spanish
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
- A minimum of 1 year of CRA experience monitoring oncology trials is required
- Must be able to travel and hold a valid driver’s license
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking an experienced Clinical Research Associate II/Sr to join our team. As a CRA, you’ll be joining a fast‑paced, driven environment that’s helping to make a life‑changing difference to patients by ensuring high‑quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams, CRAs are provided with multiple opportunities to excel and discover where their skills can take them.
Who We’re Looking For
Detail‑oriented and a strong problem solver
Highly communicative, collaborative, and adaptable
Motivated, accountable, and able to work independently
Positive, professional, and comfortable supporting virtual and in‑person teams
What You’ll Do
Monitor clinical trial sites through on‑site and remote visits
Build and maintain strong relationships with investigators and site staff
Collaborate with cross‑functional teams to meet project timelines
Manage site‑level study documentation, systems updates, and visit reports
Implement corrective actions when needed to maintain study integrity
Ensure sites are always audit- and inspection-ready
Additional Details
Home‑based role; preference for candidates residing in Mexico City
Must be fluent in English and Spanish
Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
A minimum of 1 year of CRA experience monitoring oncology trials is required
Must be able to travel and hold a valid driver’s license
Why Join Us
Be part of groundbreaking projects pushing the boundaries of clinical research
Work in a collaborative and inclusive environment that values your expertise
Unlock career growth and professional development opportunities
Enjoy work‑life balance and flexible working arrangements
If this job doesn’t sound like your next step, but you know someone who’d be a perfect fit, feel free to share this opportunity with them!
At Parexel, we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and you’re exposed to a world of experiences and open doors.
Company
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